Does TIOTROPIUM Cause Product physical issue? 807 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 807 reports of Product physical issue have been filed in association with TIOTROPIUM (Tiotropium Bromide). This represents 1.7% of all adverse event reports for TIOTROPIUM.
807
Reports of Product physical issue with TIOTROPIUM
1.7%
of all TIOTROPIUM reports
4
Deaths
63
Hospitalizations
How Dangerous Is Product physical issue From TIOTROPIUM?
Of the 807 reports, 4 (0.5%) resulted in death, 63 (7.8%) required hospitalization, and 2 (0.2%) were considered life-threatening.
Is Product physical issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TIOTROPIUM. However, 807 reports have been filed with the FAERS database.
What Other Side Effects Does TIOTROPIUM Cause?
Dyspnoea (10,863)
Incorrect route of drug administration (9,079)
Asthma (7,944)
Wheezing (5,361)
Therapeutic product effect incomplete (4,327)
Cough (4,202)
Product quality issue (3,821)
Drug ineffective (3,642)
Loss of personal independence in daily activities (3,414)
Pneumonia (3,046)
What Other Drugs Cause Product physical issue?
SUMATRIPTAN (2,349)
ICOSAPENT ETHYL (666)
LISDEXAMFETAMINE DIMESYLATE (652)
AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (387)
IBUPROFEN (337)
ESTRADIOL\LEVONORGESTREL (305)
ESTRADIOL (302)
RUXOLITINIB (302)
IXAZOMIB (298)
BUPRENORPHINE (260)
Which TIOTROPIUM Alternatives Have Lower Product physical issue Risk?
TIOTROPIUM vs TIPIRACIL\TRIFLURIDINE
TIOTROPIUM vs TIPRANAVIR
TIOTROPIUM vs TIRAGOLUMAB
TIOTROPIUM vs TIRBANIBULIN
TIOTROPIUM vs TIROFIBAN